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1. Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/ Polyposis Variant Curation Expert Panel

4. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

5. Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome.

6. Germline mutations in WNK2 could be associated with serrated polyposis syndrome.

7. Germline mutations in WNK2 could be associated with serrated polyposis syndrome

8. Wnt genes in colonic polyposis predisposition.

10. Catch them if you are aware: PTEN postzygotic mosaicism in clinically suspicious patients with PTEN Hamartoma Tumour Syndrome and literature review

11. Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort

12. Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort

13. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

15. GENOTYPE-PHENOTYPE ASSOCIATIONS PROVIDE A RATIONAL TO IDENTIFY POTENTIALLY ACTIONABLE VUS

19. Reply to Kratz et al.

20. Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes

21. Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

24. Dye chromoendoscopy leads to a higher adenoma detection in the duodenum and stomach in patients with familial adenomatous polyposis

25. Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes

33. Chromoendoskopie versus konventionelle Endoskopie im oberen Gastrointestinaltrakt bei Patienten mit familiärer adenomatöser Polyposis (ChroPol-I)

35. Distinct spectrum of apc germline mutations in familial adenomatous polyposis at the center-south of portugal: identification of a mutational hotspot and suggestion of a founder effect

37. MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events

42. F2A sequence linking MGMTP140K and MDR1 in a bicistronic lentiviral vector enables efficient chemoprotection of haematopoietic stem cells.

43. Chemoprotection of human hematopoietic stem cells by simultaneous lentiviral overexpression of multidrug resistance 1 and O6-methylguanine-DNA methyltransferaseP140K.

44. Chemoprotection of human hematopoietic stem cells by simultaneous lentiviral overexpression of multidrug resistance 1 and O6-methylguanine-DNA methyltransferaseP140K.

45. Manhattan transit with a path key

47. The Martin Mizzen

48. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

49. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

50. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

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